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A Phase 1 Dose Escalation Study of AMG 780 in Adult Subjects With Advanced Solid Tumors

This study has been terminated.
(Part A, the dose escalation and primary objective of the study, was completed. Part B, the dose expansion, was not conducted due to a business decision.)
Sponsor:
ClinicalTrials.gov Identifier:
NCT01137552
First Posted: June 4, 2010
Last Update Posted: March 4, 2015
The safety and scientific validity of this study is the responsibility of the study sponsor and investigators. Listing a study does not mean it has been evaluated by the U.S. Federal Government. Read our disclaimer for details.
Information provided by (Responsible Party):
Amgen
April 22, 2010
June 4, 2010
March 4, 2015
June 2010
December 2013   (Final data collection date for primary outcome measure)
  • To assess the safety and tolerability of AMG 780 in subjects with advanced solid malignancies (including adverse event rate, incidence of dose-limiting toxicities, and determination of maximum tolerated dose) [ Time Frame: 2.5 years ]
  • To evaluate the pharmacokinetic (PK) parameters of AMG 780 including, but not limited to Cmax, AUC, and accumulation ratio [ Time Frame: 2.5 years ]
Same as current
Complete list of historical versions of study NCT01137552 on ClinicalTrials.gov Archive Site
  • To evaluate tumor response using RECIST criteria (measured by CT/MRI) [ Time Frame: 2.5 years ]
  • To evaluate changes in tumor volume (measured by volumetric CT/MRI) [ Time Frame: 2.5 years ]
  • To evaluate changes in tumor vascularity and to estimate the relationship between dose/pharmacokinetics and vascular response (measured by DCE-MRI) [ Time Frame: 2.5 years ]
  • To evaluate the incidence of anti-AMG 780 antibody formation [ Time Frame: 2.5 years ]
Same as current
Not Provided
Not Provided
 
A Phase 1 Dose Escalation Study of AMG 780 in Adult Subjects With Advanced Solid Tumors
A Phase 1, First-in-Human Study Evaluating the Safety, Tolerability, Pharmacokinetics, and Pharmacodynamics of AMG 780 in Adult Subjects With Advanced Solid Tumors
This is a first in human, open-label, sequential dose escalation and expansion study of AMG 780 in up to 62 subjects with advanced solid tumors. The dose escalation part of the study is aimed at evaluating the safety, tolerability, pharmacokinetics and pharmacodynamics of AMG 780. The dose expansion will consist of up to 20 subjects and the dose level of AMG 780 will be dependent upon emerging safety and PK data from the dose escalation part of the study.
Not Provided
Interventional
Phase 1
Allocation: Non-Randomized
Intervention Model: Single Group Assignment
Masking: None (Open Label)
Primary Purpose: Treatment
Advanced Solid Tumors
Drug: AMG 780
AMG 780 will be administered by IV infusion every 2 weeks
  • Experimental: A
    Dose Escalation
    Intervention: Drug: AMG 780
  • Experimental: B
    Dose Expansion
    Intervention: Drug: AMG 780
Not Provided

*   Includes publications given by the data provider as well as publications identified by ClinicalTrials.gov Identifier (NCT Number) in Medline.
 
Terminated
44
April 2014
December 2013   (Final data collection date for primary outcome measure)

Inclusion Criteria:

  • Men and women ≥ 18 years old
  • Must have a pathologically documented, and definitely diagnosed, advanced solid tumor that is refractory to standard treatment, or for which no curative therapy is available, or for subjects who refuse standard therapy
  • Measurable disease by RECIST criteria
  • Must be able to undergo MRI evaluation
  • Eastern Cooperative Oncology Group (ECOG) performance status ≤ 2
  • Competent to sign and date an Institutional Review Board approved informed consent form

Exclusion Criteria:

  • Presence of untreated or symptomatic primary central nervous system tumors or metastases
  • Presence of leukemia or myelodysplastic syndrome
  • Subjects with head and neck cancer
  • Previous hematopoietic stem cell transplant (allogeneic)
  • Unresolved hematological toxicities > grade 1 with the exception of grade 2 lymphopenia and non-hematological toxicities > grade 1, excluding alopecia and grade 2 neuropathy, from prior anti-cancer therapy
  • Myocardial infarction within 1 year before study day 1, or unstable or uncontrolled disease/condition related to or affecting cardiac function
  • History of stroke, arterial or venous thrombosis, or pulmonary embolism within 1 year before study
  • Active peripheral vascular disease
  • History of bleeding diathesis
  • History of pulmonary hemorrhage or gross hemoptysis within 6 months before study
  • Known history of adrenal hemorrhage
  • Known positive test for human immunodeficiency virus infection, or active hepatitis B or hepatitis C
  • Major surgery within 1 month before study
  • Prior treatment with any agent targeting the angiopoietin-Tie2 signaling pathway
  • Concurrent antitumor treatment, except Lupron for subjects with prostate cancer and selective estrogen receptor modulators (SERMS) for subjects with breast cancer, within 4 weeks (6 weeks for nitrosoureas or mitomycin) before study day 1
  • Known sensitivity to mammalian-derived products, bacterially-produced proteins, or any of the products to be administered during dosing
  • Investigational agent within 30 days before study
  • Pregnant (eg, positive urine test) or breastfeeding
  • Subjects of childbearing potential, or subject who has a partner of childbearing potential, and is not using highly effective contraceptive precautions
Sexes Eligible for Study: All
18 Years and older   (Adult, Senior)
No
Contact information is only displayed when the study is recruiting subjects
United States
 
 
NCT01137552
20070879
No
Not Provided
Not Provided
Amgen
Amgen
Not Provided
Study Director: MD Amgen
Amgen
February 2015

ICMJE     Data element required by the International Committee of Medical Journal Editors and the World Health Organization ICTRP